🇺🇸
United States · US · US:71205-867_278d3fa3-3304-43dc-8a2a-a463c8ae9e9d
Ranolazine
Orange BookUNIISPLATC C01EB18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeC01EB18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc117120586700100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-00)
- ndc11712058673030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-30)
- ndc117120586755500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-55)
- ndc11712058676060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-60)
- ndc117120586772120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-72)
- ndc117120586778180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-78)
- ndc11712058679090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-90)
Annotations
UNII (FDA Substance ID)
A6IEZ5M406
RANOLAZINE
RxCUI 35829
Orange Book
A211829
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "A6IEZ5M406",
"rxcui": "35829",
"inchikey": "XKLMZUWKNUAPSZ-UHFFFAOYSA-N",
"display_name": "RANOLAZINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d2454377-2abd-4d9f-85f1-12f1adbb10e5": {
"match": "brand_token",
"title": "RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE [TORRENT PHARMA, INC.]",
"spl_version": "1",
"published_date": "2026-05-12"
}
},
"productid": "71205-867_278d3fa3-3304-43dc-8a2a-a463c8ae9e9d",
"productndc": "71205-867",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "211829",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Jun 4, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1GM",
"product_no": "002",
"approval_date": "Jun 4, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RANOLAZINE",
"proprietary_name": "Ranolazine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211829",
"marketing_category": "ANDA",
"nonproprietary_name": "Ranolazine",
"start_marketing_date": "20210824",
"active_numerator_strength": "500"
}Related drugs
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- CACORZYNAKYE PHARMACEUTICALS INC.
- CACORZYNAKYE PHARMACEUTICALS INC.
- DKLabigatPharmathen S.A.
- DKLabigatPharmathen S.A.
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